Think Surgical, Inc. recalls Assembly, Array Guide TMINI, REF: 109101, part of the TMINI Knee Instrument Set, used with the TMINI Miniature Robotic System
There is a galling effect (cold-weld) caused by friction between the array fixation pins and the TMINI array guide holes due to insufficient clearance between the outer diameter of the fixation pins and the inner…
Read the official notice →- Date
- 2024-03-27
- Country
- United States
- Brand
- Think Surgical
- Product
- Assembly, Array Guide TMINI, REF: 109101, part of the TMINI Knee Instrument Set, used with the TMINI Miniature Robotic System
- Classification
- Class II
- Units
- US Nationwide distribution in the states of AL, OH, NV, TX, UT, CA, MO.
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Think Surgical recalls
- 2026-07-15
USThink Surgical, Inc. recalls TMINI Femur Tracking Array REF 109003 UDI-DI code: M9461090030 TMINI Tibia Tracking Array REF 109004 UDI-DI code: M9461090040 TMINI…
Due to manufacturing/design issue where the knob on the tracking array may loosen causing potential misalignment of the array.
FDA · DeviceThink Surgical, Inc.U.S. Nationwide distribution in the states of AZ, CA, DE, FL, IA, KS, LA, MI,…Official notice →
Other drugs & medical recalls in the United States
- 2024-03-27
- US
Thommen Medical AG recalls impression coping, repositionable, short, screw-retained, PF 4.0
The depth of the internal canal was not manufactured according to specifications. Thus, the impression coping cannot be firmly connected to the implant.
FDA · DeviceThommen Medical AGUS Nationwide distribution in the states of OH and KY.Official notice → - US
Preat Corp recalls Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967
Due to a manufacturing issue, the screw seat location on the abutment product may be too high, causing mating screw to have a shorter engagement length into the associated implant.
- US
In2Bones, SAS recalls I.B.S¿ 6.5-C Compression screw - diam 6.5mm lg 80mm,Part Number S65 ST180
This Field Action is being conducted following the identification of a batch mix-up between I.B.S Compression screws diameter 6.5mm length 75mm and I.B.S Compression screws diameter 6.5mm length 80mm. The screws of the…
- US
Medtronic Inc. recalls Abre Venous Self-expanding Stent System, Product Numbers: a) AB9U14080090; b) AB9U18100090; c) AB9G14100090
There is a potential for sterile package breach.
FDA · DeviceMedtronic Inc.Worldwide distribution - US Nationwide and the countries of Australia, Canary…Official notice → - US
Medtronic Perfusion Systems recalls Medtronic DLP Vessel Cannula, Model Number REF 30000
Medtronic is writing to inform you of incorrect labeling for three manufactured lots of the DLP Vessel Cannulae for the model and lot numbers listed above.
FDA · DeviceMedtronic Perfusion SystemsUS and Brazil, Canada, Republic of Georgia, Germany, India, Ireland, Italy,…Official notice → - US
Mckesson Medical-Surgical Inc. Corporate Office recalls Steris Corporation Endo Cleaning Indicator VERIFY" RESITEST"
Facility Critical Temperature Excursions on 08-JAN 2024 in Walk-In refrigerator due to mechanical failures, causing temperatures to fall below the validated range of 35.6 - 46.4 Degrees Fahrenheit (2 - 8 Degrees…
FDA · DeviceMckesson Medical-Surgical Inc. Corporate OfficeUS Nationwide distribution in the states of AZ, PA and TX.Official notice →